HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407074Generated: October 29, 2026
Cesium carbonate → Methyl 3-{6-[(diphenylmethylene)amino]pyridazin-4-yl}benzoate
https://huagongshe.com/reaction/407074
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Methyl 3-(6-chloropyridazin-4-yl)benzoate | HCID 86667186 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 3-{6-[(diphenylmethylene)amino]pyridazin-4-yl}benzoate | HCID 86667185 | 69.6% |
Reaction Steps
A mixture of methyl 3-(6-chloropyridazin-4-yl)benzoate (0.21 g, 0.84 mmol), benzophenone imine (260 μL, 1.5 mmol), (R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (26 mg, 0.042 mmol), cesium carbonate (0.55 g, 1.7 mmol) and palladium acetate (9.5 mg, 0.042 mmol) in 1,4-dioxane (3 mL) was vacuum and refilled with nitrogen for 3 times. The reaction was stirred at 110° C. overnight. After cooling it was diluted with ethyl acetate. The organic solution was washed with water and brine, dried over Na2SO4. After filtration the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in methylene chloride (0-20%) to afford the desired product (0.23 g). LCMS (M+H)+: m/z=394.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754114B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-bc17eb2769874d5aaed9652464303362 |
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| Source note | uspto-grants-2014_06 |
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